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新型咪唑基硫代甲酰胺作为鸟嘌呤脱氨酶抑制剂

New imidazolylthiocarbamides as guanine deaminase inhibitors.

作者信息

Saxena A K, Ahmad S, Shanker K, Bhargava K P, Kishor K

出版信息

Pharmazie. 1980 Jan;35(1):16-8. doi: 10.1002/chin.198022194.

Abstract

Guanine deaminase is an important enzyme of purine catabolism which irreversibly deaminates guanine (1) to xanthine (2) and also 8-azaguanine to 8-azaxanthine. 8-Azaguanine is a carcinostatic agent whereas 8-azaxanthine is non-carcinostatic. It has been proposed that the selective action of thioguanine and 8-azaguinine on certain tissue is due to lack of guanine deaminase in these susceptible cell lines. Inhibitors of guanine deaminase are important because it is reasonable to postulate that it will inhibit the conversion of 8-azaguanine to 8-azaxanthine and these could be used with advantage along with thioguanine and 8-azaguanine. This paper reports synthesis of new imidazolylthiocarbamides as guanine deaminase inhibitors.

摘要

鸟嘌呤脱氨酶是嘌呤分解代谢中的一种重要酶,它可将鸟嘌呤(1)不可逆地脱氨生成黄嘌呤(2),同时也可将8-氮杂鸟嘌呤转化为8-氮杂黄嘌呤。8-氮杂鸟嘌呤是一种抗癌剂,而8-氮杂黄嘌呤则无抗癌作用。有人提出,硫鸟嘌呤和8-氮杂鸟嘌呤对某些组织的选择性作用是由于这些敏感细胞系中缺乏鸟嘌呤脱氨酶。鸟嘌呤脱氨酶抑制剂很重要,因为可以合理推测它将抑制8-氮杂鸟嘌呤向8-氮杂黄嘌呤的转化,并且这些抑制剂可以与硫鸟嘌呤和8-氮杂鸟嘌呤一起有利地使用。本文报道了新型咪唑基硫代甲酰胺作为鸟嘌呤脱氨酶抑制剂的合成。

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